meddevicedb.com FDA Device Reference

SPARTAN MTS

K002521 Class II Traditional
Decision Date
2000-11-13
Sponsor / Applicant
Spartan Marketing Group

Technical Specification

510(k) Submission ID K002521
Product Code ELC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4850
Decision Date 2000-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPARTAN MTS received FDA 510(k) clearance under submission number K002521, sponsored by Spartan Marketing Group. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code ELC and 21 CFR 872.4850, within the Dental review panel as a Class II device.